A methanation assembly for use with a water supply and a gas supply containing gas to be methanated in which a reactor assembly has a plurality of methanation reactors each for methanating gas input to the assembly and a gas delivery and cooling assembly adapted to deliver gas from the gas supply to each of said methanation reactors and to combine water from the water supply with the output of each methanation reactor being conveyed to a next methanation reactor and carry the mixture to such next methanation reactor.
|
1. A methanation assembly responsive to a gas supply containing gas to be methanated and a water supply comprising;
a reactor assembly including a plurality of methanation reactors each for methanating gas input to the assembly;
a gas delivery and cooling assembly adapted to deliver gas from said gas supply to each of said methanation reactors and to combine a cooling liquid comprising water from said water supply with the output of each methanation reactor being conveyed to a next methanation reactor, without cooling said output of each methanation reactor before combining said output with said cooling liquid, and to carry the mixture to such next methanation reactor.
21. An apparatus comprising:
a methanation assembly for use with a water supply and a gas supply containing gas to be methanated, said methanation assembly comprising: a reactor assembly including a plurality of methanation reactors each for methanating gas input to the assembly; and a gas delivery and cooling assembly adapted to deliver gas from said gas supply to each of said methanation reactors and to combine a cooling liquid comprising water from said water supply with the output of each methanation reactor being conveyed to a next methanation reactor without cooling said output from each methanation reactor before combining said output with said cooling liquid, and to carry the mixture to such next methanation reactor;
and a fuel cell system for receiving the output of said methanation assembly.
2. A methanation assembly in accordance with
said gas delivery and cooling assembly is further adapted to combine water from said water supply with the gas from said gas supply being delivered to the first of said methanation reactors of said plurality of methanation reactors.
3. A methanation reactor in accordance with
said gas delivery and cooling assembly is further adapted to heat said mixture of water and gas.
4. A methanation assembly in accordance with
said gas delivery and cooling assembly delivers gas from said gas supply to each next methanation reactor by adding the gas to the mixture being conveyed to said next methanation reactor one of after said mixture has been formed and as said mixture is being formed.
5. A methanation assembly according to
said gas delivery and cooling assembly comprises: one or more water injection units, each of said water injection units combining water from said water supply and the output of a methanation reactor which cools the mixture being conveyed to a next methanation reactor.
6. A methanation assembly in accordance with
said gas delivery and cooling assembly further comprises: one or more gas dividing units for dividing gas from said gas supply into a plurality of gas streams, each of said gas streams for delivery to a different one of said methanation reactors.
7. A methanation assembly in accordance with
said gas delivery and cooling assembly further comprises: one or more connecting lines, each connecting line connecting a water injection unit to a different one of said methanation reactors.
8. A methanation assembly in accordance with
each of a number of said gas streams is conveyed to a methanation reactor by delivery to one of said connecting lines.
9. A methanation assembly in accordance with
and said gas delivery and cooling assembly is further adapted to convey water from said water supply to said further connecting line.
10. A methanation assembly in accordance with
said gas delivery and cooling assembly further comprises a heat exchanger for heating the mixture of water and gas in said further connecting line.
11. A methanation assembly in. accordance with
the number of methanation reactors is three.
12. A methanation assembly in accordance with
each of a number of said gas streams is conveyed to a methanation reactor by delivery to a different one of said cooling assemblies.
13. A methanation assembly in accordance with
said gas delivery and cooling assembly further comprises: a further connecting line connected to a first of said methanation reactors of said plurality of methanation reactors, and one of said gas streams of said plurality of gas streams is conveyed to said first methanation reactor by delivery to said further connecting line;
and said gas delivery and cooling assembly is further adapted to convey water from said water supply to said further connecting line.
14. A methanation reactor in accordance with
said gas delivery and cooling assembly further comprises a heat exchanger for heating the mixture of water and gas in said further connecting line.
15. A methanation assembly in accordance with
the number of methanation reactors is three.
17. A methanation assembly in accordance with
19. A methanation assembly in accordance with
20. A methanation assembly in accordance with
said assembly comprises three methanation reactors.
22. An apparatus in accordance with
said gas delivery and cooling assembly is further adapted to combine water from said water supply with the gas from said gas supply being delivered to the first of said methanation reactors of said plurality of methanation reactors.
23. An apparatus in accordance with
said gas delivery and cooling assembly is further adapted to heat said combination of water and gas.
26. An apparatus in accordance with
27. An apparatus in accordance with
28. An apparatus in accordance with
|
This invention was made with Government support under contract DOE Contract No.: DE-FC21-95MC31262/Subcontract No. 2000-01 with Kentucky Pioneer Energy, LLC. The Government has certain rights in the invention.
This invention relates to methanation of synthesis gas and, in particular, to a methanation assembly using multiple reactors for controlled methanation.
Methanation reactions have been well known for more than 70 years and have been applied in a variety of industrial processes, including ammonia synthesis, hydrogen plant purification and production of substitute natural gas from a variety of feedstocks. Methanation is generally used as a gas purification process to remove traces of carbon oxides from gases, such as synthesis gas (“syngas”). In addition, methanation has been used to produce synthetic natural gas (methane) and can be used to convert syngas to produce methane-containing syngas suitable for use in conventional fuel cell assemblies.
Particularly, methanation of syngas involves a reaction between carbon oxides, i.e. carbon monoxide and carbon dioxide, and hydrogen in the syngas to produce methane and water, as follows:
CO+3H2→CH4+H2O (1)
CO2+4H2→CH4+2H2O (2)
Methanation reactions (1) and (2) take place at around 300° C. in a methanation reactor filled with a nickel containing catalyst and are strongly exothermic. Generally, the temperature increase in a typical methanator gas composition used in a hydrogen plant is about 74° C. for each 1% of carbon monoxide converted and 60° C. for each 1% carbon dioxide converted.
As can be appreciated, because of the exothermic nature of methanation reactions (1) and (2), the temperature in the methanation reactor during methanation of syngas has to be controlled to prevent overheating of the reactor catalyst. Also high temperatures are undesirable from an equilibrium standpoint and reduce the amount of conversion of syngas to methane since methane formation is favored at lower temperatures. Formation of soot on the reactor catalyst is also a concern and requires the addition of water to the syngas. Further, in some types of fuel cell applications, the fuel cells require that the methane reforming be done in the fuel cell stack. The endothermic methane reforming heat promotes stack heat management, reduces fresh air requirements and improves overall power plant efficiency.
Accordingly, various conventional methods have been proposed in order to control the temperature of methanation reactions. In particular, conventional assemblies using multiple methanation reactors connected in series have been used in order to limit the temperature rise during exothermic methanation reactions. For example, U.S. Pat. No. 3,967,936 teaches the use of two or more methanation reaction zones connected in series and a plurality of quench zones situated between the reaction zones such that a mixture of feed gas and cold recycle gas is delivered to the quench zones for quenching of effluent gas that emerges from each of the reaction zones. In addition, U.S. Pat. No. 4,205,961 discloses a methanation assembly for methanation of synthesis gas including two high-temperature methanation reactors connected in series followed by two low-temperature methanation reactors also connected in series. In this case, boilers and heat exchangers fed with water are used to cool through heat exchange the effluent leaving one reactor and being fed to another reactor.
Conventional methanation methods have also used multiple methanation reactors connected in series and in parallel to process two or more feed gas streams. For example, U.S. Pat. No. 4,298,694 discloses a catalytic methanation process where a feed gas rich in carbon oxides is divided into two part streams, such that the first part stream is methanated in a first methanation reactor, and the cooled effluent from the first reactor is combined with the second part stream and is methanated in a second methanation reactor. The process disclosed in the '694 patent uses a heat exchanger supplied with saturated steam to cool the effluent exiting from the first reactor.
As can be appreciated, conventional methods of controlling temperature during methanation reactions require use of complex equipment including multiple heat exchangers and gas recycling components to cool the effluent gas and to prevent overheating of the methanation reactors. Additionally, conventional methanation methods have dealt with controlling soot formation on the methanation catalyst within the methanation reactor by adding steam to the reactants going to the first reactor.
It is therefore an object of the present invention to provide a methanation assembly using multiple methanation reactors with improved temperature control to produce a gas having a desired temperature and methane composition.
It is a further object of the present invention to provide a methanation assembly using multiple methanation reactors and direct water injection as a cooling medium to control the temperature in the methanation reactors as well as to avoid deposition of soot on the methanation catalyst.
In accordance with the principles of the present invention, the above and other objectives are realized in methanation assembly for use with a water supply and a gas supply containing gas to be methanated and in which a reactor assembly has a plurality of methanation reactors each for methanating gas input to the assembly and a gas delivery and cooling assembly adapted to deliver gas from the gas supply to each of the methanation reactors and to combine water from the water supply with the output of each methanation reactor being conveyed to a next methanation reactor and to carry the mixture to such next methanation reactor. In further accord with the invention, the gas delivery and cooling assembly is further adapted to combine water from the water supply with gas from the gas supply being delivered to the first of said methanation reactors of said plurality of methanation reactors.
In the embodiment of the invention disclosed hereinbelow, three methanation reactors are employed and the gas delivery and cooling assembly includes one or more water injection units, one or more gas dividing units, one or more water routing units and connecting lines connecting these units.
The above and other features and aspects of the present invention will become more apparent upon reading the following detailed description in conjunction with the accompanying drawings, in which:
As shown, the assembly 100 comprises a methanation reactor assembly 114 which includes a series of three adiabatic methanation reactors 114A, 114B and 114C. Each of these reactors is configured to react carbon oxide and hydrogen contained in the syngas in the presence of a catalyst to produce methane and water, in accordance with the reactions (1) and (2) set forth hereinabove.
As is also shown in
In the case shown in
Each of the methanation reactors 114A-114C includes a catalyst for promoting methanation reactions between carbon oxides and hydrogen in the syngas. Although nickel catalysts are most commonly used in promoting methanation reactions, such catalysts have certain disadvantages, including, but not limited to, thermal and chemical sintering. Accordingly, in order to ensure efficient performance of the methanation assembly 100, catalysts having a high nickel concentration, i.e. greater than 50% nickel, are preferred for the reactors 114A-114C. Such catalysts are typically stable against thermal and chemical sintering during methanation of undiluted syngas streams. Alternatively, other stable catalysts which are active and selective towards methane may be used in the methanation reactors.
The gas delivery and cooling assembly 100A functions as described above by including in the assembly a syngas heater 102, first and second syngas stream dividing units 104 and 106, first and second water routing units 110 and 112, first and second water injection units 116 and 118 and connecting conduits or lines 122-146. As shown in
In the water routing unit 110, the received water is split or divided into two part water streams, i.e. a first water stream which is routed through a line 132 and a second water stream which is routed through a line 134. Similarly, syngas from the syngas supply 101 is divided by the first syngas stream dividing unit 104 into two syngas part streams. A first syngas stream is guided through a line 124 while a second syngas stream is guided through a line 126 which is coupled to the second syngas dividing unit 106.
The second syngas stream received in the second syngas dividing unit 106 is further divided by this unit into two additional streams, i.e. third and a fourth syngas streams. The third and fourth syngas streams are coupled by the dividing unit to lines 128 and 130, respectively.
Similarly, the second stream of water from the first water routing unit 110 is carried by a line 134 to the second water routing unit 112. The second water routing unit 112 further divides the second stream of water into third and a fourth water streams coupled to lines 135 and 138, respectively.
Returning to the first syngas stream traveling through the line 124, it receives the first stream of water carried through the line 132. The amount of water in this stream is determined so that a steam to carbon ratio is maintained to prevent soot formation and is a direct function of the feed or syngas stream composition. The combination of first syngas stream and first water stream then passes through the heat exchanger 102 where it is heated to approximately 500° F. and forms a mixture of syngas and steam. If the methanation assembly 100 is used in combination with a fuel cell system 120, as illustrated in
The resulting mixture of syngas and steam is carried further through the line 124 to the first methanation reactor 114A, where syngas is partially methanated by reacting a portion of the carbon oxides and hydrogen present in the syngas in the presence of a catalyst. As a result of the exothermic methanation reaction of the syngas in the first reactor 114A, the partially methanated syngas output exits the reactor 114A through a line 136 and has a temperature of approximately 1000° F.
The line 136 carries the heated partially methanated syngas output from the methanation reactor 114A to the first water injection unit 116 which also receives the third water stream in line 135. In this unit, the hot syngas output is cooled by the vaporization of the third water stream and the cooled output containing a mixture or combination of partially methanated syngas and steam is passed to the connecting line 140 which also receives the third syngas stream from the connecting line 128. It is important that the next stage syngas is added after the water injection to avoid soot formation. The third syngas stream provides more syngas reactant and also further cools this output and the resultant mixture of cooled partially methanated syngas, steam and fresh syngas at a resultant reduced temperature of approximately 450° F., is then coupled by the line 140 to the second methanation reactor 114B.
In this reactor, the mixture of methanated syngas, steam and fresh syngas is further partially methanated in the presence of a catalyst. A further partially methanated syngas output then exits the second methanation reactor 114B through a line 142 and has a temperature of approximately 1000° F.
As shown in
In the third methanation reactor 114C, the syngas and steam mixture is further methanated in the presence of a catalyst so as to convert additional carbon oxides and hydrogen present in the syngas to methane and water. Methanated syngas comprising methane and unconverted syngas exits the reactor 114C through a line 146 and has an approximate temperature of 900° F. The methanated syngas exiting from the third reactor 114C is then fed to the fuel cell system 120, where it is converted into fuel gas for the anodes of the fuel cells of the system.
In the system 100 of
As can be appreciated from the above and as shown in the examples discussed below, the inlet and outlet temperatures of the streams entering and exiting methanation reactors 114A-114C can be controlled by varying the percentage of the total fresh syngas being delivered to each of the reactors 114A-114C and the percentage of the total water being routed by the water routing units 110 and 112 to the water injection units 116 and 118. Two examples which illustrate this control are described below.
In this example, approximately one third of the total syngas delivered from the syngas supply 101 and approximately 55% of the total water from the water supply 108 are mixed and fed to the first methanation reactor 114A, at a temperature of 500° F. and a pressure of 35 psia.
Partially methanated syngas leaving the first methanation reactor 114A comprises approximately 7 mole percent of methane on a dry basis, and has a temperature of approximately about 1014° F. This partially methanated syngas is mixed in the water injection unit 116 with the third water stream comprising approximately 22.5% of the total amount of water delivered to the assembly 100. The resulting mixture of partially methanated syngas and water is cooled in the water injection unit 116, and thereafter mixed with the third syngas stream carried from the second syngas dividing unit 106. The third syngas stream comprises approximately one third of the total syngas. The resulting syngas and steam mixture is carried to the second reactor 114B and has a temperature of about 467° F.
The further methanated syngas leaving the second methanation reactor 114B comprises approximately 12 mole percent of methane on dry basis and has an outlet temperature of approximately 964° F. This partially methanated syngas is cooled in the second water injection unit 118 by adding the fourth water stream comprising approximately 22.5% of the total water delivered to the assembly 100. Before entering the third methanation reactor 114C, the mixture of partially methanated syngas and water is combined with the fourth syngas stream comprising the remainder of the total syngas delivered to the assembly, i.e. approximately one third of the total syngas. The inlet temperature of the gas mixture entering the third methanation reactor 114C is about 584° F. After undergoing methanation in the third reactor 114C, methanated syngas leaves the reactor 114C at a temperature of approximately 947° F. and has a composition of approximately 14 mole percent methane on dry basis. This syngas may then be carried to the fuel cell system 120 where it is used as fuel for the anodes of the fuel cells of the system.
In this example, syngas delivered from the syngas supply 101 is divided in the first syngas dividing unit 104 so that approximately 40% of the total syngas is delivered to the first methanation reactor 114A. The second syngas dividing unit 106 further divides the remaining 60% of the syngas equally, with 30% of the total syngas to be carried to the second methanation reactor 114B and 30% of the total syngas to be carried to the third methanation reactor 114C. Water delivered from the water supply 108 is divided by the water routing units 110 and 112 so that a mole ratio of water versus carbon (from carbon monoxide and methane) is maintained at 3.2 or higher. The maximum operating temperature of the methanation reactors 114A-114C in this example is 1002° F. and the final methane content is 15.1 vol % (dry basis).
The above-described examples of syngas and water distribution may be used in the methanation assembly arrangement of
It should be noted that the systems in the examples above were operated at low pressure consistent with the low pressure of the fuel cells. However, it is contemplated that the system of the invention can be operated at high pressures as well. High pressure operation may be preferable in certain situations as equilibrium at higher pressure favors methane production.
It should additionally be noted that while the system of
In general terms, increasing the number of reactors reduces the average reactor outlet temperature which increases the conversion of methane and reduces the amount of heat required to preheat the reactants entering the first reactor. Also, the total amount of water added is determined by the amount of water needed to avoid soot formation. In particular, to avoid soot formation, water must be added to the reaction gas in the proper ratio. This is especially important when the hot gas is passed over a catalyst which may be deactivated by soot. Therefore, all of the syngas cannot be added to the first reactor, but part of the syngas must be added after additional water is added for cooling.
Generally, the syngas is split evenly to each reactor. Additionally, the water is also split roughly evenly to each reactor, but some higher fraction of water may be added to the first reactor to control the temperatures of the reactors in the desired range.
In all cases it is understood that the above-described arrangements are merely illustrative of the many possible specific embodiments which represent applications of the present invention. For example, additional methanation reactors may be used in the methanation assembly with the syngas and water streams being further divided to provide syngas and water streams to such additional reactors. Moreover, the division of syngas and water among the reactors may be varied in order to maintain the desired temperature of the methanation reactors and the composition of the partially methanated syngas. Numerous and varied other arrangements can be readily devised in accordance with the principles of the present invention without departing from the spirit and scope of the invention.
Jahnke, Fred C., Parab, Sanjay C.
Patent | Priority | Assignee | Title |
8062799, | Aug 19 2008 | FuelCell Energy, Inc.; FUELCELL ENERGY, INC | High-efficiency dual-stack molten carbonate fuel cell system |
8236458, | Aug 19 2008 | FuelCell Energy, Inc. | High-efficiency dual-stack molten carbonate fuel cell system |
8354082, | Mar 17 2010 | Air Products and Chemicals, Inc | System for heat integration with methanation system |
9012523, | Dec 22 2011 | Kellogg Brown & Root LLC | Methanation of a syngas |
Patent | Priority | Assignee | Title |
3967936, | Jan 02 1975 | The United States of America as represented by the United States Energy | Methanation process utilizing split cold gas recycle |
3996014, | Jun 07 1974 | Metallgesellschaft Aktiengesellschaft | Methanation reactor |
4005996, | Sep 04 1975 | El Paso Natural Gas Company | Methanation process for the production of an alternate fuel for natural gas |
4016189, | Jul 27 1974 | Metallgesellschaft Aktiengesellschaft | Process for producing a gas which can be substituted for natural gas |
4028067, | Jun 10 1974 | Imperial Chemical Industries Limited | Process for producing combustible gases |
4064156, | Feb 02 1977 | UOP, DES PLAINES, IL , A NY GENERAL PARTNERSHIP; KATALISTIKS INTERNATIONAL, INC | Methanation of overshifted feed |
4133825, | May 21 1976 | British Gas PLC | Production of substitute natural gas |
4205961, | Jul 02 1977 | Metallgesellschaft | Process of producing a natural gas substitute |
4235044, | Dec 21 1978 | UOP, DES PLAINES, IL , A NY GENERAL PARTNERSHIP; KATALISTIKS INTERNATIONAL, INC | Split stream methanation process |
4298694, | Dec 12 1978 | Haldor Topsoe A/S | Process and a plant for preparing a gas rich in methane |
4525482, | Mar 23 1983 | Toyo Engineering Corporation | Process for producing a gas containing methane |
5071719, | Nov 20 1989 | Haldor Topsoe A/S | Fuel cell power plant |
5356530, | Oct 16 1992 | Method for upgrading petroleum residuum and heavy crude oil | |
6207307, | Sep 28 1996 | Johnson Matthey Public Limited Company | Carbon monoxide removal from a reformate gas |
6403049, | Sep 25 1997 | Johnson Matthey Public Limited Company | Hydrogen purification |
Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
Feb 24 2004 | JAHNKE, FRED C | FUELCELL ENERGY, INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 015184 | /0532 | |
Feb 24 2004 | PARAB, SANJAY C | FUELCELL ENERGY, INC | ASSIGNMENT OF ASSIGNORS INTEREST SEE DOCUMENT FOR DETAILS | 015184 | /0532 | |
Apr 06 2004 | FuelCell Energy, Inc. | (assignment on the face of the patent) | / | |||
Feb 10 2006 | FUEL CELL ENERGY, INC | Energy, United States Department of | CONFIRMATORY LICENSE SEE DOCUMENT FOR DETAILS | 018674 | /0671 |
Date | Maintenance Fee Events |
Jan 24 2011 | M2551: Payment of Maintenance Fee, 4th Yr, Small Entity. |
Jan 05 2015 | STOL: Pat Hldr no Longer Claims Small Ent Stat |
Jan 26 2015 | M1552: Payment of Maintenance Fee, 8th Year, Large Entity. |
Mar 11 2019 | REM: Maintenance Fee Reminder Mailed. |
Aug 26 2019 | EXP: Patent Expired for Failure to Pay Maintenance Fees. |
Date | Maintenance Schedule |
Jul 24 2010 | 4 years fee payment window open |
Jan 24 2011 | 6 months grace period start (w surcharge) |
Jul 24 2011 | patent expiry (for year 4) |
Jul 24 2013 | 2 years to revive unintentionally abandoned end. (for year 4) |
Jul 24 2014 | 8 years fee payment window open |
Jan 24 2015 | 6 months grace period start (w surcharge) |
Jul 24 2015 | patent expiry (for year 8) |
Jul 24 2017 | 2 years to revive unintentionally abandoned end. (for year 8) |
Jul 24 2018 | 12 years fee payment window open |
Jan 24 2019 | 6 months grace period start (w surcharge) |
Jul 24 2019 | patent expiry (for year 12) |
Jul 24 2021 | 2 years to revive unintentionally abandoned end. (for year 12) |